FDA Inspection 589433 — Kulzer, LLC.
The FDA completed an inspection of Kulzer, LLC. on June 23, 2009 in South Bend, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- June 23, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- South Bend, IN (United States)